Postoperative Evaluation Using Different Tourniquet Cuff Pressure in Simultaneous Bilateral Total Knee Arthroplasty -a Double-Blind Randomised Controlled Trial
Not Applicable
- Conditions
- Osteoarthritis of knee
- Registration Number
- JPRN-UMIN000029359
- Lead Sponsor
- aniwa Ikuno Hospital Joint Reconstruction Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Not provided
Exclusion Criteria
A patient who can not use tourniquet,who changed the tourniquet cuff pressure during surgery,and who judged that doctor is ineligible.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in thigh pain from preoperative to 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method Changes in thigh pain from 24 hours to 96 hours postoperatively. Changes in knee pain from preoperative to 96 hours postoperatively. Rate of the quality of the bloodless field and whether any technical difficulties had been encountered due to the quality of the bloodless field on a visual analog scale. The incidence of venous thromboembolism. Changes in knee and thigh circumference from preoperative to postoperatively. Changes in quadriceps muscle strength from preoperative to postoperatively. Changes in knee society score from preoperative to postoperatively. The incidence of complications.